Functional reconstitution of a GABAA receptor purified from bovine brain.

Article date: 1991/9/30

PubMed ID: 1656945

Journal name: Biochemical and biophysical research communications (ISSN: 0006-291X)


The GABAA/benzodiazepine receptor has been solubilized from bovine brain membranes and purified by benzodiazepine affinity chromatography. Polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulfate revealed two major protein species of 53 and 56 kDa. The purified protein has been reconstituted, in a functionally active form, into phospholipid vesicles. Chloride flux responses of the reconstituted preparations were investigated in stopped-flow experiments by monitoring fluorescence changes of a chloride-sensitive dye trapped within the vesicles. Flux was rapidly stimulated by muscimol and this response was potentiated by diazepam and blocked by desensitization of the receptor and by preincubation with the channel blocker, picrotoxin.

This document is available from: http://directlinks.cc/files/muscimol/1656945.pdf

Author List: Thuynsma R P, Dunn S M

Publication Types: Journal Article; Research Support, Non-U.S. Gov't

Substances mentioned in the article: Chloride Channels; Chlorides; Macromolecular Substances; Membrane Proteins; Receptors, GABA-A;

Mesh terms: Animals; Brain/metabolism; Cattle; Cell Membrane/metabolism; Chloride Channels; Chlorides/metabolism; Chromatography, Affinity; Electrophoresis, Polyacrylamide Gel; Kinetics; Macromolecular Substances; Membrane Proteins/metabolism; Molecular Weight; Receptors, GABA-A/isolation & purification;

1656945.txt · Last modified: 2018/11/22 21:16 (external edit)